Triphosphate oligonucleotide modification reagents and uses thereof

a technology of oligonucleotide modification and reagents, which is applied in the preparation of carboxylic acid nitrile, biochemistry apparatus and processes, organic chemistry, etc., can solve the problems of inability to prepare activated functionalities such as succinimidyl esters or maleimides, the method of oligonucleotide labelling is limited, and the label preparation is expensiv

Inactive Publication Date: 2007-02-06
VECTOR LAB +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0032]In all embodiments herein, it is preferred that one, more preferably both, of the reactive partners (e.g., the hydrazino, oxyamino or carbonyl groups) are aromatic or heteroaromatic. Thus, in preferred embodiments, the compounds of formula (I) will be aryl or heteroaryl hydrazino or oxyamino derivatives, or aryl or heteroaryl carbonyl derivatives. In more preferred embodiments, the coupling partner (e.g., the modified solid surface or the second component) will also possess an aryl or heteroaryl hydrazino or oxyamino group, or an aryl or heteroaryl carbonyl group. Hydrazone and oxime linkages formed from these preferred groups are more stable than the corresponding aliphatic hydrazone and oxime linkages, and thus are more preferred in certain applications.

Problems solved by technology

These methods of oligonucleotide labelling, however, are limited by the lack of stability of the label to the amplification reaction conditions, the inability to selectively and specifically incorporate multiple labels, and the instability of succinimidyl esters.
Preparation of activated functionalities, such as succinimidyl esters or maleimides, of labels can be costly, and not even possible in some instances, particularly under PCR conditions.

Method used

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  • Triphosphate oligonucleotide modification reagents and uses thereof
  • Triphosphate oligonucleotide modification reagents and uses thereof
  • Triphosphate oligonucleotide modification reagents and uses thereof

Examples

Experimental program
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Effect test

example 1

Synthesis of Aldehyde Triphosphate

[0264]5-Amino substituted cytidine triphosphate 5-1 was prepared from 2-deoxycytidine as described in U.S. Pat. No. 5,242,796. As shown in FIG. 5, triphosphate 5-1 was dissolved in 0.1 M phosphate, 0.15 M sodium chloride, pH 7.4 and diluted with DMF. A solution of succinimidyl 4-formylbenzoate (5-2; mmol, equiv, Pierce Chemicals, Rockford, Ill.) in DMF was added to the triphosphate. The reaction mixture was incubated at room temperature and the progress of the reaction was followed by C-18 reverse phase HPLC (mobile phase 1:50 mM triethylammbnium acetate, pH 7.4, mobile phase 2: acetonitrile; gradient: 0% 2 to 20% 2 over 20 min, 20% 2 to 50% 2 over 5 min; flow: 2 mL / min). Further reagent was added to drive the reaction to completion.

[0265]The product 5-3 was isolated by ion-exchange HPLC using DEAE-Sephadex with a gradient from water (500 mL) to 0.6 M LiCl (500 mL) as the eluting buffer. The compound was desalted by precipitation from acetone / MeOH. ...

example 2

A. Synthesis of N-(6-fluoresceinyl)-N′-(6-aminohexyl)-thiourea

[0266]As shown in FIG. 6, this compound was obtained by dissolving fluorescein isothiocyanate 6-1 (FITC)(1.03 g, 2.64 mmol) in 15 ml of MeOH in a 50 ml oven dried flask. This formed an orange suspension that was allowed to stir for 5 min at room temperature after which 1,6-diaminohexane (1.23 g, 10.56 mmol) was added all at once and the solution instantly went homogeneous. This solution was allowed to stir at room temperature for 48 hr and was covered with aluminum foil after which the reaction was completely evaporated in vacuo. The residue was dissolved in a solution of 1:1:3 EtOAc:MeOH:AcOH (4 ml). This solution was loaded onto a column packed with 61 g of silica. The column had an inner radius of 2 cm. 500 ml of 1:1:2 EtOAc:MeOH:AcOH was pushed through the column by pressure and fractions were collected and analyzed by TLC. The product 6-2 had a Rf of 0.68 and this spot was collected and evaporated to dryness followed...

example 4

Fluorescent Labeling of Aldehyde Incorporated PCR Product

[0271]Determination of incorporation of aldehyde-dCTP was performed by incubation of hydrazino-fluorescein 6-3 with Qiagen purified PCR products (from Example 3) in 0.1 M acetate, pH 5.0 for 2 hours at room temperature. The labeling reaction was terminated by addition of one volume of 0.1 M Tris-HCI, pH 7.5. The sample was purified twice with a Qiagen PCR purification kit and eluted into a final volume of 25 μL in EB buffer provided by Qiagen. Fluorescent signal was assayed by spotting 2 μl of sample onto a microscope slide (Gold Seal, Fisher Scientific) and analysis using a ScanArray Fluorescent Scanner.

[0272]

EXAMPLE 5Incorporation of aldehdye-triphosphateby a variety of enzymes using asingle-nucleotide extension assayOligonucleotideSequenceSourceM13Fcomplement5′GGGT CGT GAC TGG GAA AAC(SEQ ID NO:1)TrilinkM13FGTT TTC CCA GTC ACG AC(SEQ ID NO:2)GenosysM13RAGC CCA TAA CAA TTT CAC ACA GGA(SEQ ID NO:3)GenosysTF3AT GGA AGA ATC TCT...

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Abstract

Hydrazino, oxyamino and carbonyl-based monomers and methods for incorporation into oligonucleotides during enzymatic synthesis are provided. Modified oligonucleotides are provided that incorporate the monomers provided herein. Immobilized oligonucleotides and oligonucleotide conjugates that contain covalent hydrazone or oxime linkages are provided. Methods for preparation of surface bound oligonucleotides are provided. Methods for the preparation of oligonucleotide conjugates are also provided.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a divisional of U.S. patent application Ser. No. 09 / 630,627 filed Aug. 1, 2000 now U.S. Pat. No. 6,686,461 to Schwartz et al., entitled “TRIPHOSPHATE OLIGONUCLEOTIDE MODIFICATION REAGENTS AND USES THEREOF. “The disclosure of the above-referenced application is incorporated herein in its entirety.”FIELD OF THE INVENTION[0002]Monomers and methods for preparation, detection and immobilization of macromolecules, including biopolymers, and for preparation and detection of macromolecular conjugates are provided. The monomers for use in the methods provided herein include hydrazino, oxyamino and carbonyl substituted nucleoside triphosphates. Biopolymers, including oligonucleotides, possessing hydrazino, oxyamino or carbonyl modifications are also provided.BACKGROUND OF THE INVENTION[0003]Polymerase chain reaction (PCR) expression of oligonucleotides is a powerful tool in molecular biology. The PCR product is generally labeled...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): C07H19/04C07H19/20A61K31/70C07C253/00C07D311/88C07H19/00C07H21/00C07H21/04C12QC12Q1/68
CPCC07H19/00C07H21/04C07H21/00C07H19/04
Inventor SCHWARTZ, DAVID A.HOGREFE, RICHARD I.
Owner VECTOR LAB
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